Evaluate the Safety and Feasibility of Injecting PMD-MSC Into the Penis to Treat the Symptoms of PD

Peyronie's Disease Clinical Trial

— PMD-MSC-PD-01  

Official title:

Evaluate the Safety and Feasibility of Injecting Placental Matrix-Derived Mesenchymal Stem Cells Into the Penis to Treat the Symptoms of Peyronie's Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02395029
• Other study ID #: PMD-MSC-PD-01
• Status: Completed
• Phase: Phase 1
• First received: March 9, 2015
• Last updated: March 16, 2015
• Start date: August 2013
• Est. completion date: March 2015

Study information

• Verified date: March 2015
• Source: Z Urology
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Prospective, open labeled, non-randomized, study to be conducted at a single center. Ten subjects will undergo an injection of Placental Matrix-Derived Mesenchymal Stem Cells (PMD-MSCs) into the penis for the treatment of Peyronie's Disease. Follow up visits will be conducted at 6 weeks, 3 months, 6 months, and 12 months. Subjects will be eligible for re-injection at 3 months and/or 6 months as determined by the clinician based on patient reported treatment satisfaction.

Description:

Symptoms of Peyronie's disease include penile pain and curvature of the penis that prevents penetration and/or causes erectile dysfunction (ED). It is characterized by plaques that form along the top or bottom side of the penis inside the tunica albuginea; the plaque begins as a localized inflammation then develops into a hardened scar. Cases can range from mild to severe. In several cases, the hardened plaque reduces flexibility, causing the penis to curve during erection. The sexual problems as a result can lower a man's self-esteem and interfere with a couple's physical and emotional relationship.

The cause is unknown; however, possibilities include trauma, inherited conditions, Vitamin E deficiency, diabetes, and vascular disease.

Conservative treatments used in the acute phase (initial onset of symptoms) include oral therapies. Vitamin E and antioxidants can decrease the build-up of harmful chemicals that can cause injury to tissue. It is often used as the traditional treatment; it is inexpensive and with proper dosing, there are minimal side effects. Other oral agents include Potaba (aminobenzoates potassium); however, it is expensive ($1000 per year) and has associated gastrointestinal side effects.

Other therapies involve injections directly in the plaques (intralesional) with chemicals such as collagenase or calcium-channel blockers.

Surgical therapies are offered once the disease is stable (symptoms present for one year). Invasive surgical options consist of correction of the penile curvature or the placement of a penile prosthesis to straighten the penis to allow for erections.

Mesenchymal stem cells (MSCs) have been used for a variety of medical treatments to repair and regenerate acute and chronically damaged tissues. These cells have the potential to repair human tissue by forming cells of mesenchymal origin, such as cartilage, bone, fat, muscle, and blood vessels. Most research has focused on bone marrow derived stem cells (BMC) however the process for harvesting the cells is invasive, painful, and yields a low cell count. The human placenta offers an alternative source form MSCs. Placental Matrix-Derived Mesenchymal Stem Cells (PMD-MSCs) are compromised of a novel cellular repair matrix derived from placental mesenchyme. Mesenchyme is the meshwork of embryonic connective tissue in the mesoderm, from which are formed the muscular and connective tissues of the body and also the blood vessels. PMD-MSCs provide the extracellular matrix viable mesenchymal stem cells (MSCs) that coordinate the tissue repair process, regenerative growth factors, and anti-inflammatory cytokines required to regenerate the damaged vasculature of the penile corpora.

The research proposed here will establish the safety and feasibility of utilizing intracavernosal, intralesional injections of PMD-MSCs to treat Peyronie's disease with the intent of avoiding surgery.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: March 2015
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. acquired penile curvature >15 and <90 degrees associated with palpable penile plaque on physical examination

2. 1 or 2 penile plaque at screening

Exclusion Criteria:

1. taking the medication Coumadin

2. unable to achieve adequate erection with penile injection to access degree of curvature

3. undergone definitive treatment for prostate cancer, bladder cancer, or other pelvic malignancies including surgery, external beam radiation therapy, brachytherapy, cryotherapy

4. prior history of prostate cancer, hematologic disorders, chronic liver disease including cirrhosis and hepatitis C, disorders affecting the immune system, including infection with the human immunodeficiency virus, or psychiatric disorder including major depression, schizophrenia, bipolar disease

5. history of cerebrovascular accident, history of deep venous thrombosis within the past 5 years or history of untreated or severe sleep apnea

6. clinically significant abnormal lab results that would put the subject at increased risk or compromise the integrity of the study data, in the opinion of the investigator

7. received any other investigational drug within 30 days

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Penile Induration
• Peyronie's Disease

Intervention

Biological:
• Placental Matrix-Derived Mesenchymal Stem Cells (PMD-MSCs)

Locations

Country	Name	City	State
United States	Z Urology	Coral Springs	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Melissa Marchand

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Peak Systolic Velocity with trimix (cm/s)		Baseline	No
Other	Peak Systolic Velocity with trimix (cm/s)		6 weeks	No
Other	Peak Systolic Velocity with trimix (cm/s)		3 months	No
Other	Peak Systolic Velocity with trimix (cm/s)		6 months	No
Other	Peak Systolic Velocity with trimix (cm/s)		12 months	No
Other	End Diastolic Velocity with trimix (cm/s)		Baseline	No
Other	End Diastolic Velocity with trimix (cm/s)		6 weeks	No
Other	End Diastolic Velocity with trimix (cm/s)		3 months	No
Other	End Diastolic Velocity with trimix (cm/s)		6 months	No
Other	End Diastolic Velocity with trimix (cm/s)		12 months	No
Other	Rigidity test (Pass or Fail)		Baseline	No
Other	Rigidity test (Pass or Fail)		6 weeks	No
Other	Rigidity test (Pass or Fail)		3 months	No
Other	Rigidity test (Pass or Fail)		6 months	No
Other	Rigidity test (Pass or Fail)		12 months	No
Other	Stretched Penile Length before trimix (cm/s)		Baseline	No
Other	Stretched Penile Length before trimix (cm/s)		6 weeks	No
Other	Stretched Penile Length before trimix (cm/s)		3 months	No
Other	Stretched Penile Length before trimix (cm/s)		6 months	No
Other	Stretched Penile Length before trimix (cm/s)		12 months	No
Other	Post Penile Width with trimix		Baseline	No
Other	Post Penile Width with trimix		6 weeks	No
Other	Post Penile Width with trimix		3 months	No
Other	Post Penile Width with trimix		6 months	No
Other	Post Penile Width with trimix		12 months	No
Other	International Index of Erectile Function (IIEF)		Baseline	No
Other	International Index of Erectile Function (IIEF)		6 weeks	No
Other	International Index of Erectile Function (IIEF)		3 months	No
Other	International Index of Erectile Function (IIEF)		6 months	No
Other	International Index of Erectile Function (IIEF)		12 months	No
Other	#1 Penile Plaque (Location) Size (mm^3)		Baseline	No
Other	#1 Penile Plaque (Location) Size (mm^3)		6 weeks	No
Other	#1 Penile Plaque (Location) Size (mm^3)		3 months	No
Other	#1 Penile Plaque (Location) Size (mm^3)		6 months	No
Other	#1 Penile Plaque (Location) Size (mm^3)		12 months	No
Other	#2 Penile Plaque (Location) Size (mm^3)		Baseline	No
Other	#2 Penile Plaque (Location) Size (mm^3)		6 weeks	No
Other	#2 Penile Plaque (Location) Size (mm^3)		3 months	No
Other	#2 Penile Plaque (Location) Size (mm^3)		6 months	No
Other	#2 Penile Plaque (Location) Size (mm^3)		12 months	No
Other	#3 Penile Plaque (Location)Size (mm^3)		Baseline	No
Other	#3 Penile Plaque (Location)Size (mm^3)		6 weeks	No
Other	#3 Penile Plaque (Location)Size (mm^3)		3 months	No
Other	#3 Penile Plaque (Location)Size (mm^3)		6 months	No
Other	#3 Penile Plaque (Location)Size (mm^3)		12 months	No
Other	Penile Curvature Angle (degrees)		Baseline	No
Other	Penile Curvature Angle (degrees)		6 weeks	No
Other	Penile Curvature Angle (degrees)		3 months	No
Other	Penile Curvature Angle (degrees)		6 months	No
Other	Penile Curvature Angle (degrees)		12 months	No
Primary	Peak Systolic Velocity without trimix (cm/s)		Baseline	No
Primary	Peak Systolic Velocity without trimix (cm/s)		6 weeks	No
Primary	Peak Systolic Velocity without trimix (cm/s)		3 months	No
Primary	Peak Systolic Velocity without trimix (cm/s)		6 months	No
Primary	Peak Systolic Velocity without trimix (cm/s)		12 months	No
Secondary	End Diastolic Velocity without trimix (cm/s)		Baseline	No
Secondary	End Diastolic Velocity without trimix (cm/s)		6 weeks	No
Secondary	End Diastolic Velocity without trimix (cm/s)		3 months	No
Secondary	End Diastolic Velocity without trimix (cm/s)		6 months	No
Secondary	End Diastolic Velocity without trimix (cm/s)		12 months	No